CY1114058T1 - METHOD OF PREPARING OPTIONALLY PURE ACTIVE COMPOUNDS - Google Patents
METHOD OF PREPARING OPTIONALLY PURE ACTIVE COMPOUNDSInfo
- Publication number
- CY1114058T1 CY1114058T1 CY20131100012T CY131100012T CY1114058T1 CY 1114058 T1 CY1114058 T1 CY 1114058T1 CY 20131100012 T CY20131100012 T CY 20131100012T CY 131100012 T CY131100012 T CY 131100012T CY 1114058 T1 CY1114058 T1 CY 1114058T1
- Authority
- CY
- Cyprus
- Prior art keywords
- active compounds
- pure active
- preparing optionally
- optionally pure
- preparing
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrrole Compounds (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pyridine Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Η εφεύρεση σχετίζεται με μια νέα μέθοδο παρασκευής οπτικώς καθαρών PPI οι οποίοι έχουν δομή σουλφινυλίου με χρήση χειρόμορφου συμπλόκου ζιρκονίου ή χειρόμορφου συμπλόκου αφνίου.The invention relates to a novel method of making optically pure PPIs having a sulfinyl structure using a chiral zirconium complex or chiral hafnium complex.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02027273 | 2002-12-06 | ||
| DE10340255 | 2003-08-29 | ||
| EP03782288A EP1578742B1 (en) | 2002-12-06 | 2003-12-03 | Process for preparing optically pure active compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1114058T1 true CY1114058T1 (en) | 2016-07-27 |
Family
ID=32509784
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY20131100012T CY1114058T1 (en) | 2002-12-06 | 2013-01-07 | METHOD OF PREPARING OPTIONALLY PURE ACTIVE COMPOUNDS |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US7452998B2 (en) |
| EP (1) | EP1578742B1 (en) |
| JP (1) | JP4612542B2 (en) |
| KR (1) | KR101062806B1 (en) |
| CN (1) | CN100482658C (en) |
| AR (1) | AR042277A1 (en) |
| AU (1) | AU2003289948B2 (en) |
| BR (2) | BRPI0310118B1 (en) |
| CA (1) | CA2507807C (en) |
| CY (1) | CY1114058T1 (en) |
| DK (1) | DK1578742T3 (en) |
| EA (1) | EA011771B1 (en) |
| ES (1) | ES2397380T3 (en) |
| HK (1) | HK1078864A1 (en) |
| HR (1) | HRP20050604B1 (en) |
| IL (1) | IL168456A (en) |
| IS (1) | IS2885B (en) |
| ME (1) | ME00563A (en) |
| MX (1) | MXPA05005762A (en) |
| NO (1) | NO330978B1 (en) |
| NZ (1) | NZ540815A (en) |
| PL (1) | PL375818A1 (en) |
| PT (1) | PT1578742E (en) |
| RS (1) | RS52667B (en) |
| SI (1) | SI1578742T1 (en) |
| TW (1) | TWI313268B (en) |
| WO (1) | WO2004052882A1 (en) |
| ZA (1) | ZA200503543B (en) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000041698A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS |
| EP1575941B1 (en) | 2002-12-06 | 2012-04-11 | Nycomed GmbH | Process for preparing (S)-pantoprazole |
| FR2848555B1 (en) * | 2002-12-16 | 2006-07-28 | Negma Gild | ENANTIOMER (-) OF TENATOPRAZOLE AND ITS THERAPEUTIC APPLICATION |
| CA2510849A1 (en) * | 2002-12-19 | 2004-07-08 | Teva Pharmaceutical Industries Ltd | Solid states of pantoprazole sodium, processes for preparing them and processes for preparing known pantoprazole sodium hydrates |
| CA2528993A1 (en) * | 2003-06-10 | 2004-12-23 | Teva Pharmaceutical Industries Ltd. | Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole |
| CA2568652A1 (en) * | 2004-06-02 | 2005-12-15 | Altana Pharma Ag | Process for the preparation of pyridin-2-ylmethylsulphinyl-1h-benzimidazol compounds |
| FR2871800B1 (en) * | 2004-06-17 | 2006-08-25 | Sidem Pharma Sa Sa | SODIUM SALT S-TENATOPRAZOLE MONOHYDRATE AND THERAPEUTIC APPLICATION |
| WO2006001753A1 (en) * | 2004-06-24 | 2006-01-05 | Astrazeneca Ab | New process for the preparation of crystal modifications for use in the preparation of esomeprazole sodium salt |
| EP1801110A1 (en) | 2005-12-22 | 2007-06-27 | KRKA, tovarna zdravil, d.d., Novo mesto | Esomeprazole arginine salt |
| US7579476B2 (en) * | 2006-02-24 | 2009-08-25 | Praktikatalyst Pharma, Llc | Transition metal mediated oxidation of hetero atoms in organic molecules coordinated to transition metals |
| US8173818B2 (en) | 2006-08-08 | 2012-05-08 | Jubilant Organosys Limited | Process for producing sulphoxide compounds |
| WO2008047681A1 (en) | 2006-10-13 | 2008-04-24 | Eisai R & D Management Co., Ltd. | Benzimidazole compound having gastric acid secretion inhibitory activity |
| AU2007317561A1 (en) | 2006-10-27 | 2008-05-15 | The Curators Of The University Of Missouri | Compositions comprising at least one acid labile proton pump inhibiting agents, optionally other pharmaceutically active agents and methods of using same |
| CN101977909A (en) * | 2008-03-18 | 2011-02-16 | 雷迪博士实验室有限公司 | Dexlansoprazole process and polymorphs |
| EP2143722A1 (en) | 2008-07-09 | 2010-01-13 | Lek Pharmaceuticals D.D. | Process for preparation of esomeprazole sodium of high chemical purity and new forms of esomeprazole sodium |
| EP2264024A1 (en) | 2008-10-14 | 2010-12-22 | LEK Pharmaceuticals d.d. | Process for the preparation of enantiomerically enriched proton pump inhibitors |
| US8071781B2 (en) | 2008-11-11 | 2011-12-06 | Syn-Tech Chem. & Pharm. Co., Ltd. | Process for preparing rabeprazole sodium |
| CN102770423B (en) | 2010-02-12 | 2014-10-15 | 埃斯特维化学股份有限公司 | Preparation process of the sodium salt of esomeprazole |
| CN103113351B (en) * | 2013-03-08 | 2015-01-21 | 苏州特瑞药业有限公司 | Method for preparing optically pure chiral sulfoxide compound |
| CN103936714A (en) * | 2014-04-15 | 2014-07-23 | 北京华禧联合科技发展有限公司 | Preparation method of esomeprazole magnesium |
| EP3239146A4 (en) | 2014-12-26 | 2018-05-30 | The University of Tokyo | Method for producing proton pump inhibitor compound having optical activity |
| CN105440018A (en) * | 2015-11-27 | 2016-03-30 | 福州闽海药业有限公司 | Asymmetric oxidation synthesis method of zirconium-catalyzed dexlansoprazole |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE7804231L (en) | 1978-04-14 | 1979-10-15 | Haessle Ab | Gastric acid secretion |
| IL75400A (en) | 1984-06-16 | 1988-10-31 | Byk Gulden Lomberg Chem Fab | Dialkoxypyridine methyl(sulfinyl or sulfonyl)benzimidazoles,processes for the preparation thereof and pharmaceutical compositions containing the same |
| JPS6150978A (en) | 1984-08-16 | 1986-03-13 | Takeda Chem Ind Ltd | Pyridine derivative and preparation thereof |
| FI90544C (en) | 1986-11-13 | 1994-02-25 | Eisai Co Ltd | Process for Preparation as Drug Useful 2-Pyridin-2-yl-methylthio- and sulfinyl-1H-benzimidazole derivatives |
| SE465514B (en) | 1990-02-19 | 1991-09-23 | Curt Pettersson | PROCEDURE AND APPLICATION OF A SEPARATION MEDIUM FOR SEANT Separation |
| DE4035455A1 (en) | 1990-11-08 | 1992-05-14 | Byk Gulden Lomberg Chem Fab | ENANTIOMER SEPARATION |
| WO1994025028A1 (en) | 1993-04-27 | 1994-11-10 | Sepracor, Inc. | Methods and compositions for treating gastric disorders using optically pure (+) pantoprazole |
| JPH08509736A (en) | 1993-04-27 | 1996-10-15 | セプラコー，インコーポレイテッド | Methods and compositions for treating gastric disorders using optically pure (-) pantoprazole |
| SE9301830D0 (en) | 1993-05-28 | 1993-05-28 | Ab Astra | NEW COMPOUNDS |
| SE504459C2 (en) | 1994-07-15 | 1997-02-17 | Astra Ab | Process for the preparation of substituted sulfoxides |
| GB9423968D0 (en) | 1994-11-28 | 1995-01-11 | Astra Ab | Resolution |
| GB9423970D0 (en) | 1994-11-28 | 1995-01-11 | Astra Ab | Oxidation |
| HRP960232A2 (en) | 1995-07-03 | 1998-02-28 | Astra Ab | A process for the optical purification of compounds |
| EP1575941B1 (en) | 2002-12-06 | 2012-04-11 | Nycomed GmbH | Process for preparing (S)-pantoprazole |
-
2003
- 2003-12-03 EP EP03782288A patent/EP1578742B1/en not_active Expired - Lifetime
- 2003-12-03 CA CA2507807A patent/CA2507807C/en not_active Expired - Fee Related
- 2003-12-03 ES ES03782288T patent/ES2397380T3/en not_active Expired - Lifetime
- 2003-12-03 DK DK03782288.9T patent/DK1578742T3/en active
- 2003-12-03 US US10/536,766 patent/US7452998B2/en not_active Expired - Fee Related
- 2003-12-03 EA EA200500898A patent/EA011771B1/en not_active IP Right Cessation
- 2003-12-03 BR BRPI0310118A patent/BRPI0310118B1/en not_active IP Right Cessation
- 2003-12-03 BR BR0317005-5A patent/BR0317005A/en unknown
- 2003-12-03 ME MEP-848/08A patent/ME00563A/en unknown
- 2003-12-03 SI SI200332234T patent/SI1578742T1/en unknown
- 2003-12-03 RS YU20050423A patent/RS52667B/en unknown
- 2003-12-03 MX MXPA05005762A patent/MXPA05005762A/en active IP Right Grant
- 2003-12-03 PL PL03375818A patent/PL375818A1/en not_active Application Discontinuation
- 2003-12-03 JP JP2005502310A patent/JP4612542B2/en not_active Expired - Fee Related
- 2003-12-03 WO PCT/EP2003/013605 patent/WO2004052882A1/en active Application Filing
- 2003-12-03 PT PT37822889T patent/PT1578742E/en unknown
- 2003-12-03 NZ NZ540815A patent/NZ540815A/en not_active IP Right Cessation
- 2003-12-03 AR ARP030104447A patent/AR042277A1/en unknown
- 2003-12-03 CN CNB2003801044100A patent/CN100482658C/en not_active Expired - Fee Related
- 2003-12-03 AU AU2003289948A patent/AU2003289948B2/en not_active Ceased
- 2003-12-03 KR KR1020057009778A patent/KR101062806B1/en not_active Expired - Fee Related
- 2003-12-05 TW TW092134409A patent/TWI313268B/en not_active IP Right Cessation
-
2005
- 2005-05-04 ZA ZA200503543A patent/ZA200503543B/en unknown
- 2005-05-05 IL IL168456A patent/IL168456A/en not_active IP Right Cessation
- 2005-06-23 IS IS7909A patent/IS2885B/en unknown
- 2005-06-24 NO NO20053099A patent/NO330978B1/en not_active IP Right Cessation
- 2005-06-29 HR HRP20050604AA patent/HRP20050604B1/en not_active IP Right Cessation
- 2005-11-28 HK HK05110824.6A patent/HK1078864A1/en not_active IP Right Cessation
-
2013
- 2013-01-07 CY CY20131100012T patent/CY1114058T1/en unknown
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